Granzyme B ELISPOT assay for ex vivo measurements of T cell immunity

被引:79
作者
Rininsland, FH
Helms, T
Asaad, RJ
Boehm, BO
Tary-Lehmann, M
机构
[1] Case Western Reserve Univ, Sch Med, Inst Pathol, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Dept Infect Dis, Cleveland, OH 44106 USA
[3] Univ Hosp Ulm, Endocrinol Sect, D-89081 Ulm, Germany
关键词
ELISPOT; granzyme B; cytotoxic T cells; memory; peptide-specificity;
D O I
10.1016/S0022-1759(00)00191-5
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A major goal in immunodiagnostics has been the development of assay systems that can measure CD8(-) T cell immunity in humans, directly ex vivo, at high resolution, and with high throughput. We established granzyme B (grB) enzyme-linked immunospot assay (ELISPOT) in conjunction with image analysis to this end. Using grB transfected and untransfected Chinese hamster ovary (CHO) cells and T cell lines, we show that the antibody pair utilized was grB-specific and that only activated T cells secrete grB. GrB release began within 4 h after antigen stimulation and stopped within 40 h. Side-by-side comparison showed grB ELISPOT assays to have a higher resolution than classic chromium-release assays in terms of signal-to-noise ratio. The linearity of the relation of the number of CD8(+) effector T cells plated to grB spots detected suggests that grB ELISPOT assays measure the frequencies of grB-secreting cells directly. Reactivity to HIV peptides was seen in grB ELISPOT assays of freshly isolated PBMC from HIV patients, consistent with the detection of peptide-specific memory cells. The higher resolution and lower labor and material investment should make grB ELISPOT assays an attractive alternative to chromium-release assays in monitoring the clonal sizes of specific CD8 memory cells in vivo. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:143 / 155
页数:13
相关论文
共 23 条
  • [1] Phenotypic analysis of antigen-specific T lymphocytes
    Altman, JD
    Moss, PAH
    Goulder, PJR
    Barouch, DH
    McHeyzerWilliams, MG
    Bell, JI
    McMichael, AJ
    Davis, MM
    [J]. SCIENCE, 1996, 274 (5284) : 94 - 96
  • [2] STRUCTURE, FUNCTION, AND DIVERSITY OF CLASS-I MAJOR HISTOCOMPATIBILITY COMPLEX-MOLECULES
    BJORKMAN, PJ
    PARHAM, P
    [J]. ANNUAL REVIEW OF BIOCHEMISTRY, 1990, 59 : 253 - 288
  • [3] Single cell analyses of cytokine production
    Carter, LL
    Swain, SL
    [J]. CURRENT OPINION IN IMMUNOLOGY, 1997, 9 (02) : 177 - 182
  • [4] Dissecting the multifactorial causes of immunodominance in class I-restricted T cell responses to viruses
    Chen, WS
    Antón, LC
    Bennink, JR
    Yewdell, JW
    [J]. IMMUNITY, 2000, 12 (01) : 83 - 93
  • [5] ENGELHARD VH, 1994, ANNU REV IMMUNOL, V12, P181, DOI 10.1146/annurev.immunol.12.1.181
  • [6] ALLELE-SPECIFIC MOTIFS REVEALED BY SEQUENCING OF SELF-PEPTIDES ELUTED FROM MHC MOLECULES
    FALK, K
    ROTZSCHKE, O
    STEVANOVIC, S
    JUNG, G
    RAMMENSEE, HG
    [J]. NATURE, 1991, 351 (6324) : 290 - 296
  • [7] CYTOKINE-SPECIFIC ELISPOT ASSAY - SINGLE CELL ANALYSIS OF IL-2, IL-4 AND IL-6 PRODUCING CELLS
    FUJIHASHI, K
    MCGHEE, JR
    BEAGLEY, KW
    MCPHERSON, DT
    MCPHERSON, SA
    HUANG, CM
    KIYONO, H
    [J]. JOURNAL OF IMMUNOLOGICAL METHODS, 1993, 160 (02) : 181 - 189
  • [8] GRABSTEIN K, 1980, SELECTED METHODS CEL, P124
  • [9] THE CELL BIOLOGY OF CTL KILLING
    GRIFFITHS, GM
    [J]. CURRENT OPINION IN IMMUNOLOGY, 1995, 7 (03) : 343 - 348
  • [10] Identification of LFA-1 as a candidate autoantigen in treatment-resistant Lyme arthritis
    Gross, DM
    Forsthuber, T
    Tary-Lehmann, M
    Etling, C
    Ito, K
    Nagy, ZA
    Field, JA
    Steere, AC
    Huber, BT
    [J]. SCIENCE, 1998, 281 (5377) : 703 - 706